Linked Data
gnomAD v4:
20-2470807-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.2470807G>T , CM000682.2:g.2470807G>T | GRCh38 |
| NC_000020.10:g.2451453G>T , CM000682.1:g.2451453G>T | GRCh37 |
| NC_000020.9:g.2399453G>T | NCBI36 |
| NG_042057.1:g.5047C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000339610.10:c.-117C>A | ENSP00000342305.7:n.-117C>A | |
| ENST00000381342.6:c.-117C>A | ENSP00000370746.2:n.-117C>A | |
| ENST00000438552.6:c.-117C>A | ENSP00000412566.2:n.-117C>A | |
| ENST00000461548.1:c.305-3049C>A | ENSP00000456213.1:n.305-3049C>A | |
| NM_003091.3:c.-117C>A | NP_003082.1:n.-117C>A | |
| NM_198216.1:c.-117C>A | NP_937859.1:n.-117C>A |